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February 28, 2012 — Cambridge Consultants will demonstrate new Bluetooth low energy (BLE) iPhone 4S applications using CSR’s BLE devices at this year’s Mobile World Congress in Barcelona.

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Jarvik Heart Inc. announced conditional U.S. Food and Drug Administration (FDA) approval of its pivotal trial for evaluation of the Jarvik 2000 heart for destination therapy (DT). Use of the device for DT means that it will provide long-term, permanent support to end-stage congestive heart failure patients who are not candidates for heart transplant.

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Boston Scientific Corp. announces the first implants of a Teligen implantable cardioverter-defibrillator (ICD) in China. The implants were performed by Farong Shen, M.D., in Zhejiang Hospital, Hangzhou and Wei Hua, M.D., in Fuwai Hospital, Beijing. The Teligen family of ICDs, designed to treat sudden cardiac death, are the smallest and thinnest high-energy devices available in China.

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Avinger Inc. announced the enrollment of the first European patient in the CONNECT II global clinical trial. The first patient was enrolled by Dr. Bernhard Reimers at Ospedale di Mirano in Mirano, Italy.

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Subject to its devices receiving necessary U.S. Food and Drug Administration (FDA) approvals, Boston Scientific Corp. will have the capability to transmit implantable cardiac device data to physicians and other healthcare providers in North America across the AT&T wireless network in the future, AT&T announced.

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The U.S. Department of Health and Human Services (HHS) announced the next steps for providers who are using electronic health record (EHR) technology and receiving incentive payments from Medicare and Medicaid. These proposed rules, from the Centers for Medicaid and Medicaid Services (CMS) and the Office of the National Coordinator for Health Information Technology (ONC), will govern Stage 2 of the Medicare and Medicaid Electronic Health Record Incentive Programs.

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February 24, 2012 — Hospital readmissions continue to be a challenge nationwide. It has been estimated that chronic diseases such as asthma, congestive heart failure (CHF) and diabetes account for over 80 percent of hospital inpatient stays. CHF alone is the leading cause of hospital admissions for Americans over the age of 65.

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February 24, 2012 — TeraRecon Inc. highlighted the capability of its flagship iNtuition enterprise image management solution to image-enable the electronic medical record (EMR) at the annual meeting of the Healthcare Information and Management Systems Society (HIMSS), held Feb. 21-23, 2012, at the Las Vegas Sands Expo.

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February 24, 2012 — A new imaging efficiency measure developed by the Centers for Medicare and Medicaid Services (CMS) to reduce computed tomography (CT) scans in emergency departments does not accurately determine which hospitals are performing CT scans inappropriately, according to a new study published online Annals of Emergency Medicine (“Assessment of Medicare's Imaging Efficiency Measure for Emergency Department Patients with Atraumatic Headache”).

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February 24, 2012 — 3-D Surgical Solutions LLC and Wheaton Franciscan-The Wisconsin Heart Hospital Campus announced that the first case ever using the Leonardo 3-D vision system was successfully conducted in a surgical robotic procedure.

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February 24, 2012 — CardioInsight Technologies Inc. announced that it has successfully completed the European commercial introduction of its ECVUE system to aid in the diagnosis of cardiac arrhythmias.

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February 24, 2012 — A new report released today by HealthGrades found that from 2008 to 2010, emergency admissions for heart attack decreased slightly (1.7 percent) for Medicare patients, but admissions for stroke increased by 2.2 percent.

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February 24, 2012 — Positron Corp., through its wholly owned subsidiary, Manhattan Isotope Technology LLC (MIT), announced it had received its first shipment of strontium-82 (Sr-82) from the ARRONAX Cyclotron Facility in Nantes, France.

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The Centers for Medicare and Medicaid Services (CMS) yesterday released its proposed rule regarding Stage 2 meaningful use (MU) of electronic medical records (EMRs). The Office of the National Coordinator for Health IT (ONC) is expected to publish the associated standards, implementation specifications and certification criteria in the next couple days. Both proposals will be published in the Federal Register on March 7 with 60-day public comment periods.

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February 24, 2012 — CardioFocus Inc., developer of the HeartLight Endoscopic Ablation System (EAS) for the treatment of atrial fibrillation (AF), announced the first patient has been enrolled and treated in the HeartLight EAS U.S. pivotal trial, designed to evaluate the safety and efficacy of the technology in treating symptomatic AF.

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